Enzyme Nanoreactor for In Vivo Detoxification of Organophosphates
T.N Pashirova
1
,
Zukhra Shaihutdinova
1, 2
,
Milana Mansurova
2
,
Renata Kazakova
2
,
Dinara Shambazova
2
,
Andrei Bogdanov
1
,
Dmitry Tatarinov
1
,
David Daudé
3
,
Pauline Jacquet
3
,
Eric Chabrière
3, 4
,
Patrick Masson
2
3
Gene&GreenTK, 19−21 Boulevard Jean Moulin, Marseille 13005, France
|
Publication type: Journal Article
Publication date: 2022-04-19
scimago Q1
wos Q1
SJR: 1.921
CiteScore: 14.5
Impact factor: 8.2
ISSN: 19448244, 19448252
PubMed ID:
35440137
General Materials Science
Abstract
A nanoreactor containing an evolved mutant of Saccharolobus solfataricus phosphotriesterase (L72C/Y97F/Y99F/W263V/I280T) as a catalytic bioscavenger was made for detoxification of organophosphates. This nanoreactor intended for treatment of organophosphate poisoning was studied against paraoxon (POX). Nanoreactors were low polydispersity polymersomes containing a high concentration of enzyme (20 μM). The polyethylene glycol-polypropylene sulfide membrane allowed for penetration of POX and exit of hydrolysis products. In vitro simulations under second order conditions showed that 1 μM enzyme inactivates 5 μM POX in less than 10 s. LD50-shift experiments of POX-challenged mice through intraperitoneal (i.p.) and subcutaneous (s.c.) injections showed that intravenous administration of nanoreactors (1.6 nmol enzyme) protected against 7 × LD50i.p. in prophylaxis and 3.3 × LD50i.p. in post-exposure treatment. For mice s.c.-challenged, LD50 shifts were more pronounced: 16.6 × LD50 in prophylaxis and 9.8 × LD50 in post-exposure treatment. Rotarod tests showed that transitory impaired neuromuscular functions of challenged mice were restored the day of experiments. No deterioration was observed in the following days and weeks. The high therapeutic index provided by prophylactic administration of enzyme nanoreactors suggests that no other drugs are needed for protection against acute POX toxicity. For post-exposure treatment, co-administration of classical drugs would certainly have beneficial effects against transient incapacitation.
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Total citations:
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Citations from 2024:
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(52.63%)
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GOST
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Pashirova T. et al. Enzyme Nanoreactor for In Vivo Detoxification of Organophosphates // ACS applied materials & interfaces. 2022. Vol. 14. No. 17. pp. 19241-19252.
GOST all authors (up to 50)
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Pashirova T., Shaihutdinova Z., Mansurova M., Kazakova R., Shambazova D., Bogdanov A., Tatarinov D., Daudé D., Jacquet P., Chabrière E., Masson P. Enzyme Nanoreactor for In Vivo Detoxification of Organophosphates // ACS applied materials & interfaces. 2022. Vol. 14. No. 17. pp. 19241-19252.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/acsami.2c03210
UR - https://doi.org/10.1021/acsami.2c03210
TI - Enzyme Nanoreactor for In Vivo Detoxification of Organophosphates
T2 - ACS applied materials & interfaces
AU - Pashirova, T.N
AU - Shaihutdinova, Zukhra
AU - Mansurova, Milana
AU - Kazakova, Renata
AU - Shambazova, Dinara
AU - Bogdanov, Andrei
AU - Tatarinov, Dmitry
AU - Daudé, David
AU - Jacquet, Pauline
AU - Chabrière, Eric
AU - Masson, Patrick
PY - 2022
DA - 2022/04/19
PB - American Chemical Society (ACS)
SP - 19241-19252
IS - 17
VL - 14
PMID - 35440137
SN - 1944-8244
SN - 1944-8252
ER -
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BibTex (up to 50 authors)
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@article{2022_Pashirova,
author = {T.N Pashirova and Zukhra Shaihutdinova and Milana Mansurova and Renata Kazakova and Dinara Shambazova and Andrei Bogdanov and Dmitry Tatarinov and David Daudé and Pauline Jacquet and Eric Chabrière and Patrick Masson},
title = {Enzyme Nanoreactor for In Vivo Detoxification of Organophosphates},
journal = {ACS applied materials & interfaces},
year = {2022},
volume = {14},
publisher = {American Chemical Society (ACS)},
month = {apr},
url = {https://doi.org/10.1021/acsami.2c03210},
number = {17},
pages = {19241--19252},
doi = {10.1021/acsami.2c03210}
}
Cite this
MLA
Copy
Pashirova, T.N, et al. “Enzyme Nanoreactor for In Vivo Detoxification of Organophosphates.” ACS applied materials & interfaces, vol. 14, no. 17, Apr. 2022, pp. 19241-19252. https://doi.org/10.1021/acsami.2c03210.